Substance P plays a critical role in synaptic transmission in striatal neurons

Substance P is one of the major neuropeptides released by striatal neurons; however, its function in the striatum remains unclear. In this study, we found substance P triggers spontaneous neurotransmitter release and rapid synaptic vesicle exocytosis in cultured striatal neurons, as substance P knoc...

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Published inBiochemical and biophysical research communications Vol. 511; no. 2; pp. 369 - 373
Main Authors He, Zi-Xuan, Liu, Ting-Yu, Yin, Yue-Yue, Song, Hui-Fang, Zhu, Xiao-Juan
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 02.04.2019
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Abstract Substance P is one of the major neuropeptides released by striatal neurons; however, its function in the striatum remains unclear. In this study, we found substance P triggers spontaneous neurotransmitter release and rapid synaptic vesicle exocytosis in cultured striatal neurons, as substance P knockdown in these neurons impaired spontaneous neurotransmitter release and calcium-dependent rapid synaptic neurotransmission. Furthermore, treatment with exogenous substance P completely rescued the synaptic dysfunction phenotype in striatal neurons lacking this neuropeptide. On the other hand, substance P knockdown had no effect on the size of the readily releasable pool of synaptic vesicles, but decreased the probability of presynaptic release of synaptic vesicles in cultured striatal neurons. Treatment with CP96345, a NK1 receptor antagonist, also resulted in synaptic defects in cultured striatal neurons. In summary, we propose substance P is critical for synaptic transmission in striatal neurons. •Substance P knockdown in striatal neurons impairs spontaneous release.•Diminished rapid synaptic transmission in striatal neurons lacking substance P.•Substance P is critical for the regulation of the probability of presynaptic release in striatal neurons.•NK1 receptors is important for the modulation of synaptic transmission by substance P.
AbstractList Substance P is one of the major neuropeptides released by striatal neurons; however, its function in the striatum remains unclear. In this study, we found substance P triggers spontaneous neurotransmitter release and rapid synaptic vesicle exocytosis in cultured striatal neurons, as substance P knockdown in these neurons impaired spontaneous neurotransmitter release and calcium-dependent rapid synaptic neurotransmission. Furthermore, treatment with exogenous substance P completely rescued the synaptic dysfunction phenotype in striatal neurons lacking this neuropeptide. On the other hand, substance P knockdown had no effect on the size of the readily releasable pool of synaptic vesicles, but decreased the probability of presynaptic release of synaptic vesicles in cultured striatal neurons. Treatment with CP96345, a NK1 receptor antagonist, also resulted in synaptic defects in cultured striatal neurons. In summary, we propose substance P is critical for synaptic transmission in striatal neurons.
Substance P is one of the major neuropeptides released by striatal neurons; however, its function in the striatum remains unclear. In this study, we found substance P triggers spontaneous neurotransmitter release and rapid synaptic vesicle exocytosis in cultured striatal neurons, as substance P knockdown in these neurons impaired spontaneous neurotransmitter release and calcium-dependent rapid synaptic neurotransmission. Furthermore, treatment with exogenous substance P completely rescued the synaptic dysfunction phenotype in striatal neurons lacking this neuropeptide. On the other hand, substance P knockdown had no effect on the size of the readily releasable pool of synaptic vesicles, but decreased the probability of presynaptic release of synaptic vesicles in cultured striatal neurons. Treatment with CP96345, a NK1 receptor antagonist, also resulted in synaptic defects in cultured striatal neurons. In summary, we propose substance P is critical for synaptic transmission in striatal neurons. •Substance P knockdown in striatal neurons impairs spontaneous release.•Diminished rapid synaptic transmission in striatal neurons lacking substance P.•Substance P is critical for the regulation of the probability of presynaptic release in striatal neurons.•NK1 receptors is important for the modulation of synaptic transmission by substance P.
Author He, Zi-Xuan
Song, Hui-Fang
Zhu, Xiao-Juan
Liu, Ting-Yu
Yin, Yue-Yue
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  surname: He
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Keywords Striatum
NK1 receptor
Substance p
Synaptic transmission
Language English
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Snippet Substance P is one of the major neuropeptides released by striatal neurons; however, its function in the striatum remains unclear. In this study, we found...
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SubjectTerms Animals
Cells, Cultured
Corpus Striatum - cytology
Corpus Striatum - metabolism
Mice
Neurons - cytology
Neurons - metabolism
NK1 receptor
Presynaptic Terminals - metabolism
Striatum
Substance p
Substance P - metabolism
Synaptic Transmission
Synaptic Vesicles - metabolism
Title Substance P plays a critical role in synaptic transmission in striatal neurons
URI https://dx.doi.org/10.1016/j.bbrc.2019.02.055
https://www.ncbi.nlm.nih.gov/pubmed/30803756
https://search.proquest.com/docview/2186146017
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